咪唑-4-乙醛
外观
(重定向自C5H6N2O)
咪唑-4-乙醛 | |
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别名 | 1H-Imidazole-5-acetaldehyde, 1H-Imidazole-5-acetaldehyde, Imidazole-4-acetaldehyde, 1H-Imidazole-4-acetaldehyde, Imidazole-5-acetaldehyde, 4-Imidazolylacetaldehyde, 2-(1H-Imidazol-4-yl)acetaldehyde, 2-(1H-Imidazol-5-yl)acetaldehyde |
识别 | |
CAS号 | 645-14-7 ![]() |
PubChem | 150841 |
ChemSpider | 132948 |
SMILES |
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InChI |
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InChIKey | MQSRGWNVEZRLDK-UHFFFAOYSA-N |
ChEBI | 27398 |
KEGG | C05130 |
性质 | |
化学式 | C5H6N2O |
摩尔质量 | 110.11 g·mol⁻¹ |
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 |
咪唑-4-乙醛或咪唑-5-乙醛是一种有机氮化合物,化学式为C5H6N2O,它是组胺的代谢产物。它可以被NAD依赖性乙醛脱氢酶进一步氧化,生成咪唑-4-乙酸。[1][2]
参考文献
[编辑]- ^ Bähre H, Kaever V. Analytical Methods for the Quantification of Histamine and Histamine Metabolites. Handb Exp Pharmacol. Handbook of Experimental Pharmacology. 2017, 241: 3–19. ISBN 978-3-319-58192-7. PMID 28321587. doi:10.1007/164_2017_22.
- ^ Ambroziak W, Maśliński C. Participation of aldehyde dehydrogenase in the oxidative deamination pathway of histamine and putrescine. Agents Actions. April 1988, 23 (3–4): 311–3. PMID 3394581. S2CID 8283492. doi:10.1007/BF02142573.